Evidence map›Paper›PMID 27565575›Full record

ArticleBMC bioinformatics2016

Statistical inference for time course RNA-Seq data using a negative binomial mixed-effect model.

Xiaoxiao Sun, David Dalpiaz, Di Wu, Jun S Liu, Wenxuan Zhong, Ping Ma

Abstract read
In one paragraph

Article in BMC bioinformatics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. A Survey of Statistical Methods for Microbiome Data Analysis.Frontiers in applied mathematics and statistics · 2022
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Xiaoxiao SunDepartment of Statistics, University of Georgia, 101 Cedar Street, Athens, 30602, USA.
David DalpiazDepartment of Statistics, University of Illinois at Urbana-Champaign, 725 South Wright Street, Champaign, 61820, USA.
Di WuDepartment of Statistics, Harvard University, One Oxford Street, Cambridge, 02138, USA.
Jun S LiuDepartment of Statistics, Harvard University, One Oxford Street, Cambridge, 02138, USA.
Wenxuan ZhongDepartment of Statistics, University of Georgia, 101 Cedar Street, Athens, 30602, USA.
Ping MaDepartment of Statistics, University of Georgia, 101 Cedar Street, Athens, 30602, USA. pingma@uga.edu.

Funding

Novel statistical tools for cell line specific epigenetic analysisR01GM113242 · NIGMS · UNIVERSITY OF GEORGIA · PI ZHONG, WENXUAN · 2014 to 2017
$1.4M
Deciphering the Regulatory Role of Small RNAs on Alternative Splicing R01GM122080 · NIGMS · UNIVERSITY OF GEORGIA · PI MA, PING · 2016 to 2019
$1.3M
NIGMS NIH HHS R01 GM113242NIGMS NIH HHS R01 GM122080
6 · The paper itself

Abstract

backgroundAccurate identification of differentially expressed (DE) genes in time course RNA-Seq data is crucial for understanding the dynamics of transcriptional regulatory network. However, most of the available methods treat gene expressions at different time points as replicates and test the significance of the mean expression difference between treatments or conditions irrespective of time. They thus fail to identify many DE genes with different profiles across time. In this article, we propose a negative binomial mixed-effect model (NBMM) to identify DE genes in time course RNA-Seq data. In the NBMM, mean gene expression is characterized by a fixed effect, and time dependency is described by random effects. The NBMM is very flexible and can be fitted to both unreplicated and replicated time course RNA-Seq data via a penalized likelihood method. By comparing gene expression profiles over time, we further classify the DE genes into two subtypes to enhance the understanding of expression dynamics. A significance test for detecting DE genes is derived using a Kullback-Leibler distance ratio. Additionally, a significance test for gene sets is developed using a gene set score.

resultsSimulation analysis shows that the NBMM outperforms currently available methods for detecting DE genes and gene sets. Moreover, our real data analysis of fruit fly developmental time course RNA-Seq data demonstrates the NBMM identifies biologically relevant genes which are well justified by gene ontology analysis.

conclusionsThe proposed method is powerful and efficient to detect biologically relevant DE genes and gene sets in time course RNA-Seq data.

Indexed as

Models, StatisticalAnimalsDrosophilaLikelihood FunctionsRNASequence Analysis, RNARNAAnalysis of varianceDifferentially expressed geneGene set enrichmentPenalized likelihoodSmoothing spline

Identifiers

PMID27565575
PMCPMC5002174

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.